Variant report

Variant	rs6920832
Chromosome Location	chr6:119689056-119689057
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 91 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:88)

rs_ID	r²[population]
rs1022869	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1022870	0.93[ASN][1000 genomes]
rs1028327	0.86[ASN][1000 genomes]
rs1028328	0.86[ASN][1000 genomes]
rs10456921	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10457352	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10457353	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10457355	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10457356	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10485001	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10872173	0.86[ASN][1000 genomes]
rs10872177	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11153796	0.93[ASN][1000 genomes]
rs11153797	0.93[ASN][1000 genomes]
rs11153800	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs11153803	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11153805	1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11153808	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11153810	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11153811	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11153812	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11751945	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs11755967	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11759899	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11961647	0.93[ASN][1000 genomes]
rs11962938	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12192420	0.93[ASN][1000 genomes]
rs12198423	0.93[ASN][1000 genomes]
rs12198667	0.93[ASN][1000 genomes]
rs12199883	0.81[ASN][1000 genomes]
rs12200554	0.86[ASN][1000 genomes]
rs12205260	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12205826	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12206472	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12207595	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12524617	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12527248	0.81[ASN][1000 genomes]
rs1295383	0.81[ASN][1000 genomes]
rs1295384	0.81[ASN][1000 genomes]
rs1295388	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1797067	0.81[ASN][1000 genomes]
rs2036257	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs2092218	0.86[ASN][1000 genomes]
rs2144236	0.81[ASN][1000 genomes]
rs35305935	0.81[ASN][1000 genomes]
rs4607463	0.86[ASN][1000 genomes]
rs56827721	0.92[ASN][1000 genomes]
rs61094987	0.92[ASN][1000 genomes]
rs6569056	0.86[ASN][1000 genomes]
rs6569057	0.86[ASN][1000 genomes]
rs6569065	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6569066	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6569072	1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs6569073	0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6569076	0.81[ASN][1000 genomes]
rs6903249	0.93[ASN][1000 genomes]
rs6909928	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6913626	0.93[ASN][1000 genomes]
rs6913654	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6915957	0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6918913	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs6932241	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6932292	0.86[ASN][1000 genomes]
rs6935126	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6936790	0.81[ASN][1000 genomes]
rs73529045	1.00[ASN][1000 genomes]
rs73529086	1.00[ASN][1000 genomes]
rs73535209	0.84[ASN][1000 genomes]
rs73535254	0.84[ASN][1000 genomes]
rs7740993	0.86[ASN][1000 genomes]
rs7743824	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7745295	0.81[ASN][1000 genomes]
rs7745633	0.81[ASN][1000 genomes]
rs7750041	0.93[ASN][1000 genomes]
rs7750901	1.00[JPT][hapmap]
rs7750941	1.00[JPT][hapmap]
rs7753492	0.93[ASN][1000 genomes]
rs7754482	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7760582	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7763569	0.86[ASN][1000 genomes]
rs7767198	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7770398	1.00[JPT][hapmap]
rs7770777	0.93[ASN][1000 genomes]
rs926859	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9374795	0.81[ASN][1000 genomes]
rs9481900	1.00[JPT][hapmap]
rs9489669	1.00[JPT][hapmap]
rs9489697	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025995	chr6:119407742-119709548	Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	esv3447598	chr6:119558591-120119384	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	esv3389526	chr6:119558598-120190087	ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:119671800-119689200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr6:119673400-119690000	Weak transcription	K562	blood
3	chr6:119677000-119691800	Weak transcription	Adipose Nuclei	Adipose
4	chr6:119679400-119691600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr6:119681000-119690200	Weak transcription	Primary T cells from cord blood	blood
6	chr6:119682000-119693200	Weak transcription	Left Ventricle	heart
7	chr6:119688000-119689200	Enhancers	Fetal Heart	heart
8	chr6:119688200-119689200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr6:119688600-119690200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr6:119688800-119701400	Weak transcription	Primary B cells from cord blood	blood
11	chr6:119689000-119691200	Weak transcription	Brain Anterior Caudate	brain
12	chr6:119689000-119693400	Weak transcription	Primary hematopoietic stem cells	blood

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